Evidence map›Paper›PMID 41779159›Full record

ArticlePediatric surgery international2026

Assessment of quality of life in patients with Müllerian anomalies at a referral center in Colombia.

Daniela Moreno Villamizar, Tatiana Daza Ladino, Maria Jose Neira, Fernando Fierro, Juan Valero

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Article in Pediatric surgery international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Daniela Moreno VillamizarDepartment of Pediatric Surgery, Universidad Nacional de Colombia, Bogotá, Colombia. mmorenovi@unal.edu.co.
Tatiana Daza LadinoMedical Physician, Universidad de ciencias aplicadas y ambientales , Bogotá, Colombia.
Maria Jose NeiraMedical Physician, Universidad El Bosque, Bogotá, Colombia.
Fernando FierroPediatric Surgeon, HOMI-Fundación Hospital Pediátrico La Misericordia, Universidad Nacional de Colombia, Bogotá, Colombia.
Juan ValeroPediatric Surgeon, HOMI-Fundación Hospital Pediátrico La Misericordia, Universidad Nacional de Colombia, Bogotá, Colombia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate quality of life in pediatric patients with Müllerian anomalies who underwent surgical intervention between 2018 and 2023.

methodsA retrospective descriptive case series was conducted including patients younger than 18 years who underwent surgical correction for Müllerian anomalies between 2018 and 2023. Quality of life was assessed using the validated Spanish version of the Pediatric Quality of Life Inventory (PedsQL 4.0

resultsThe most frequent anomalies were longitudinal vaginal septum and uterus didelphys (42.8%), while OHVIRA syndrome was least common (2.9%). Renal agenesis occurred in 28.6% of patients, predominantly right-sided (80%), and anorectal malformations (ARM) were associated in 57.1%. All underwent vaginoscopy and surgery, most commonly vaginal septum resection (40%). The PedsQL was applied by phone to all patients, with a mean follow-up of 48 months. Mean quality-of-life scores were good and comparable between parent-proxy and self-reports in the 13-18-year (73.34 vs. 77.51) and 8-12-year (68.75 vs. 72.82) groups. The highest scores were in the 2-4-year (80.43) and 5-7-year (79.71) groups. Emotional functioning consistently scored lowest, while physical and social functioning were highest. Currently, 25.7% of patients have initiated sexual activity, and two have had children-one by vaginal delivery and one by cesarean.

conclusionsPediatric patients with Müllerian anomalies demonstrated good postoperative quality of life, highlighting the positive impact of timely surgical management on physical, social, and reproductive outcomes.

Indexed as

Congenital AbnormalitiesMullerian DuctsQuality of LifeAdolescentChildChild, PreschoolColombiaFemaleHumansInfantRetrospective StudiesUterusVaginaMüllerian anomaliesPediatric surgeryPedsQLQuality of lifeReproductive outcomes

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.